International safety notice
IntelliVue Patient Monitor
Swiss / SwissMedic · CHE · Jul 26, 2010
Key facts
| Title | IntelliVue Patient Monitor |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | IntelliVue Patient Monitor |
| Manufacturer | Philips Medical Systems |
| Models | M8000-9024x, M8000-9023x, M8000-9002x, M8000-9021x, M8000-9017x, 使用说明书》（M8000-9013x）提供补充信息：, M8000-9016x, DE22701289, MP20-MP90, ユーザーズ・ガイド』（M8000-9010x）の内容を補足するものです。本書は上記ユーザーズ・ガイドと併せて保管し、必要に応じて参照してください。, M8000-9011x, DE84399581 and 36 more |
| Event type | Safety Notice |
| Date | Jul 26, 2010 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1